chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	120733420	120733421	T	A	31	GENIC	possibly homozygous	111689064
3	120735447	120735448	A	T	34	GENIC	homozygous	111689065
3	120736087	120736088	T	C	60	GENIC	homozygous	111689066
3	120736466	120736467	A	G	37	GENIC	homozygous	111689067
3	120736650	120736651	T	C	67	GENIC	homozygous	111689068
3	120736894	120736895	A	G	50	GENIC	homozygous	111689069
3	120737212	120737213	G	A	49	GENIC	homozygous	111689070
3	120737267	120737268	A	G	47	GENIC	homozygous	111689071
3	120737442	120737443	G	A	50	GENIC	heterozygous	111689072
3	120737948	120737949	A	G	64	GENIC	homozygous	111689073
3	120737959	120737960	C	G	70	GENIC	homozygous	111689074
3	120738337	120738338	A	G	32	GENIC	homozygous	111689075
3	120738494	120738495	G	A	67	GENIC	homozygous	111689076
3	120738767	120738768	C	T	57	GENIC	homozygous	111689077
3	120745982	120745983	G	A	46	GENIC	homozygous	111689078
3	120749917	120749918	T	C	40	GENIC	homozygous	111689079
3	120751897	120751898	T	G	42	GENIC	homozygous	111689080
3	120754107	120754108	A	G	33	GENIC	homozygous	111689081
3	120757679	120757680	A	G	47	GENIC	homozygous	111689082
3	120759532	120759533	A	T	38	GENIC	heterozygous	111689083
3	120760976	120760977	C	G	51	GENIC	homozygous	111689084
3	120761493	120761494	G	A	23	GENIC	possibly homozygous	111689085
3	120763480	120763481	A	G	50	GENIC	possibly homozygous	111689086